Literature DB >> 29052159

Recommended Methods for the Collection of Health State Utility Value Evidence in Clinical Studies.

Roberta Ara1, John Brazier2, Tracey Young1.   

Abstract

A conceptual model framework and an initial literature review are invaluable when considering what health state utility values (HSUVs) are required to populate health states in decision models. They are the recommended starting point early within a research and development programme, and before development of phase III trial protocols. While clinical trials can provide an opportunity to collect the required evidence, their appropriateness should be reviewed against the requirements of the model structure taking into account population characteristics, time horizon and frequency of clinical events. Alternative sources such as observational studies or registries may be more appropriate when evidence describing changes in HSUVs over time or rare clinical events is required. Phase IV clinical studies may provide the opportunity to collect additional longitudinal real-world evidence. Aspects to consider when designing the collection of the evidence include patient and investigator burden, whom to ask, the representativeness of the population, the exact definitions of health states within the economic model, the timing of data collection, sample size, and mode of administration. Missing data can be an issue, particularly in longitudinal studies, and it is important to determine whether the missing data will bias inferences from analyses. For example, respondents may fail to complete follow-up questionnaires because of a relapse or the severity of their condition. The decision on the preferred study type and the particular quality of life measure should be informed by any evidence currently available in the literature, the design of data collection, and the exact requirements of the model that will be used to support resource allocation decisions (e.g. reimbursement).

Entities:  

Mesh:

Year:  2017        PMID: 29052159     DOI: 10.1007/s40273-017-0549-6

Source DB:  PubMed          Journal:  Pharmacoeconomics        ISSN: 1170-7690            Impact factor:   4.981


  31 in total

1.  Self-reported health: reliability and consequences for health inequality measurement.

Authors:  Philip M Clarke; Chris Ryan
Journal:  Health Econ       Date:  2006-06       Impact factor: 3.046

2.  Estimating Health-State Utility for Economic Models in Clinical Studies: An ISPOR Good Research Practices Task Force Report.

Authors:  Sorrel E Wolowacz; Andrew Briggs; Vasily Belozeroff; Philip Clarke; Lynda Doward; Ron Goeree; Andrew Lloyd; Richard Norman
Journal:  Value Health       Date:  2016 Sep - Oct       Impact factor: 5.725

3.  Mapping to Estimate Health-State Utility from Non-Preference-Based Outcome Measures: An ISPOR Good Practices for Outcomes Research Task Force Report.

Authors:  Allan J Wailoo; Monica Hernandez-Alava; Andrea Manca; Aurelio Mejia; Joshua Ray; Bruce Crawford; Marc Botteman; Jan Busschbach
Journal:  Value Health       Date:  2017-01       Impact factor: 5.725

Review 4.  The Role of Condition-Specific Preference-Based Measures in Health Technology Assessment.

Authors:  Donna Rowen; John Brazier; Roberta Ara; Ismail Azzabi Zouraq
Journal:  Pharmacoeconomics       Date:  2017-12       Impact factor: 4.981

Review 5.  Health-related quality of life and symptom reporting: similarities and differences between children and their parents.

Authors:  Christine Eiser; James W Varni
Journal:  Eur J Pediatr       Date:  2013-05-29       Impact factor: 3.183

6.  The Swedish early psoriatic arthritis register-- 2-year followup: a comparison with early rheumatoid arthritis.

Authors:  Ulla R C Lindqvist; Gerd-Marie Alenius; Tomas Husmark; Elke Theander; Gunilla Holmström; Per T Larsson
Journal:  J Rheumatol       Date:  2008-02-15       Impact factor: 4.666

7.  Estimating utility values for health states of type 2 diabetic patients using the EQ-5D (UKPDS 62).

Authors:  Philip Clarke; Alastair Gray; Rury Holman
Journal:  Med Decis Making       Date:  2002 Jul-Aug       Impact factor: 2.583

8.  The management of acute venous thromboembolism in clinical practice - study rationale and protocol of the European PREFER in VTE Registry.

Authors:  Giancarlo Agnelli; Anselm K Gitt; Rupert Bauersachs; Eva-Maria Fronk; Petra Laeis; Patrick Mismetti; Manuel Monreal; Stefan N Willich; Wolf-Peter Wolf; Alexander T Cohen
Journal:  Thromb J       Date:  2015-10-21

9.  The effect of diabetes complications on health-related quality of life: the importance of longitudinal data to address patient heterogeneity.

Authors:  Maria Alva; Alastair Gray; Borislava Mihaylova; Philip Clarke
Journal:  Health Econ       Date:  2013-07-11       Impact factor: 3.046

10.  How people with multiple sclerosis rate their quality of life: an EQ-5D survey via the UK MS register.

Authors:  Kerina H Jones; David V Ford; Philip A Jones; Ann John; Rodden M Middleton; Hazel Lockhart-Jones; Jeffrey Peng; Lisa A Osborne; J Gareth Noble
Journal:  PLoS One       Date:  2013-06-11       Impact factor: 3.240

View more
  1 in total

1.  The Impact of Hypoglycemia on Productivity Loss and Utility in Patients With Type 2 Diabetes Treated With Insulin in Real-world Canadian Practice: Protocol for a Prospective Study.

Authors:  Veronique Lambert-Obry; Jean-Philippe Lafrance; Michelle Savoie; Jean Lachaine
Journal:  JMIR Res Protoc       Date:  2022-03-28
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.